Canonical Allele Identifier: CA2160364125
Gene: BAG5 HGNC NCBI

Linked Data

dbSNP Id: rs7693

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.103557367C>A , CM000676.2:g.103557367C>A GRCh38
NC_000014.8:g.104023704C>A , CM000676.1:g.104023704C>A GRCh37
NC_000014.7:g.103093457C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000299204.6:c.*2454G>T MANE Select ENSP00000299204.4:n.*2454G>T
ENST00000299204.4:c.*2454G>T ENSP00000299204.4:n.*2454G>T
ENST00000445922.2:c.*2454G>T ENSP00000391713.2:n.*2454G>T
NM_001015048.2:c.*2454G>T NP_001015048.1:n.*2454G>T
NM_001015049.2:c.*2454G>T NP_001015049.1:n.*2454G>T
NM_004873.3:c.*2454G>T NP_004864.1:n.*2454G>T
NM_001015049.3:c.*2454G>T NP_001015049.1:n.*2454G>T
NM_004873.4:c.*2454G>T NP_004864.1:n.*2454G>T
NM_001015048.3:c.*2454G>T MANE Select NP_001015048.1:n.*2454G>T
NM_001015049.5:c.*2454G>T NP_001015049.2:n.*2454G>T